Venous Thrombosis
Conditions
Brief summary
To determine the effect of an interventional campaign run by a dedicated VTE Nurse Educator over a 6-month period and the effect on prophylaxis rates. To determine the proportion of medically admitted patients with risk factors for VTE. To assess and compare the use of venous thromboembolism (VTE) prophylaxis in hospitalized medical patients versus recommendations and current guidelines. To determine the patient characteristics of those deemed to be at risk of VTE. To determine the proportion of patients receiving appropriate thromboprophylaxis for their risk. To determine the type and duration (where possible) of prophylaxis used.
Interventions
None listed
Sponsors
Sanofi
Study design
Observational model
CASE_ONLY
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Hospital admission for an acute illness with an in-patient hospital stay of 3 days or more.
Exclusion criteria
* Patients who have undergone any type of surgery during current admission * Patients who are admitted to a ward or department that is excluded from this study e.g psychiatric, paediatric, maternity, intensive care unit, coronary care unit. * Prior enrollment in this protocol during current admission * Prior enrollment in a VTE study involving pharmaceutical or mechanical treatment within last 90 days. * Admission for suspected or diagnosed deep vein thrombosis The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Countries
Australia
Outcome results
None listed